Canonical Allele Identifier: PA101263
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 373948
ClinVar RCV Id: RCV000415091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Arg90Cys
CA16043593
NM_000266.4:c.268C>T